Phellodenol B

Details

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Internal ID c511b174-5d87-4a17-b2b3-b27bd81c53a7
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 7-hydroxycoumarins
IUPAC Name 7-hydroxy-8-(2-hydroxyethyl)chromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H10O4/c12-6-5-8-9(13)3-1-7-2-4-10(14)15-11(7)8/h1-4,12-13H,5-6H2
InChI Key SWKJRSKBKHLXMA-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O4
Molecular Weight 206.19 g/mol
Exact Mass 206.05790880 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.03
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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612086-87-0
2H-1-Benzopyran-2-one, 7-hydroxy-8-(2-hydroxyethyl)-
7-hydroxy-8-(2-hydroxyethyl)chromen-2-one
RefChem:172566

2D Structure

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2D Structure of Phellodenol B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9071 90.71%
Caco-2 + 0.5377 53.77%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8043 80.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8355 83.55%
OATP1B3 inhibitior + 0.9239 92.39%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9172 91.72%
P-glycoprotein inhibitior - 0.9735 97.35%
P-glycoprotein substrate - 0.9666 96.66%
CYP3A4 substrate - 0.6976 69.76%
CYP2C9 substrate - 0.5981 59.81%
CYP2D6 substrate - 0.8001 80.01%
CYP3A4 inhibition - 0.8646 86.46%
CYP2C9 inhibition - 0.7253 72.53%
CYP2C19 inhibition - 0.6605 66.05%
CYP2D6 inhibition - 0.8367 83.67%
CYP1A2 inhibition - 0.6948 69.48%
CYP2C8 inhibition - 0.8280 82.80%
CYP inhibitory promiscuity - 0.8783 87.83%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6639 66.39%
Eye corrosion - 0.9927 99.27%
Eye irritation + 0.9659 96.59%
Skin irritation - 0.7559 75.59%
Skin corrosion - 0.9668 96.68%
Ames mutagenesis - 0.5337 53.37%
Human Ether-a-go-go-Related Gene inhibition - 0.8199 81.99%
Micronuclear - 0.5367 53.67%
Hepatotoxicity + 0.5658 56.58%
skin sensitisation - 0.8613 86.13%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.5857 58.57%
Acute Oral Toxicity (c) III 0.4124 41.24%
Estrogen receptor binding - 0.6432 64.32%
Androgen receptor binding + 0.6665 66.65%
Thyroid receptor binding - 0.7074 70.74%
Glucocorticoid receptor binding + 0.6636 66.36%
Aromatase binding + 0.5519 55.19%
PPAR gamma + 0.6910 69.10%
Honey bee toxicity - 0.9469 94.69%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity + 0.6791 67.91%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.30% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 93.16% 83.82%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 89.22% 86.92%
CHEMBL2581 P07339 Cathepsin D 86.90% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.24% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.25% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.97% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.87% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 81.69% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Phellodendron chinense var. glabriusculum

Cross-Links

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PubChem 11745794
NPASS NPC223632
LOTUS LTS0239667
wikiData Q105262725